Duns Number:025460908
Device Description: SwabFlush®
Catalog Number
711-600
Brand Name
Excelsior
Version/Model Number
711-600
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
Yes
For Single-Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K130975,K130975,K130975
Product Code
NGT
Product Code Name
Saline, vascular access flush
Public Device Record Key
badab3a0-bfb3-4aff-873b-bb9e9d744c1a
Public Version Date
September 16, 2022
Public Version Number
4
DI Record Publish Date
September 24, 2016
Package DI Number
20363807000005
Quantity per Package
6
Contains DI Package
10363807000008
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 38540 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 85094 |
| 3 | A medical device with high risk that requires premarket approval | 2 |
| U | Unclassified | 7 |